Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled for Device Malfunction
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
- Product
- Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF IAB-06850-U
- Category
- Medical Device
- Distribution
- Distributed nationwide